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NCT07750275Enrolling by invitation

Safety and Economics of Parenchymal Transection in Minimally Invasive Liver Surgery

Safety and Economics of Parenchymal Transection in Minimally Invasive Liver Surgery (LIVER-MIND 2): a Multicentre Retrospective Registry of the Italian Society of Endoscopic Surgery (SICE)

Source: ClinicalTrials.gov · Last updated 6 Aug 2026

Brief summary (registry, in English)

LIVER-MIND 2 is a multicentre, observational, retrospective registry coordinated by the SICE HPB and Minimally Invasive Surgery Working Group, enrolling consecutive adults undergoing elective minimally invasive (laparoscopic, robotic or hybrid) liver resection between January 2021 and December 2025 across ≥15 high-volume or dedicated centres (target \>30 centres).

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
800 (estimated)
First submitted
20 Jul 2026
Start date
1 Jan 2021
Primary completion date
Dec 2026
Lead sponsor
University of Molise
NCT number
NCT07750275

What you commit to

  • Study type: Observational
  • Planned participants: 800
  • From 1 Jan 2021 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Urgent or emergency surgery
  • Liver transplantation (donor / recipient)
  • Associated major non-hepatic biliary or vascular resection
  • Surgery before January 2021

Other

  • Lack of consent or follow-up
  • Participation in conflicting interventional trials
  • Robotic procedures performed during the learning-curve phase (first 65 robotic cases per centre, per Rahimli et al.)

Who the study is looking for

  • Age ≥ 18 years
  • Elective minimally invasive liver resection
  • Laparoscopic, robotic or hybrid approach
  • Benign or malignant disease
  • Signed informed consent for use of anonymised data
  • Data completeness ≥ 70% in the CRF

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Molise
Coordinator of this site? Confirm its status
CampobassoItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.